ClinGen Allele Registry
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Canonical Allele Identifier:
CA414793734
Gene: MT-CO2
HGNC
NCBI
Linked Data
MyVariant Identifiers:
chrMT:g.7787C>A (hg38)
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Genomic Alleles
HGVS
Genome Assembly
NC_012920.1:m.7787C>A , J01415.2:m.7787C>A
GRCh38
Transcript Alleles
HGVS
Amino-acid Change
ENST00000361739.1:c.202C>A
ENSP00000354876.1:p.Leu68Met
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